E2 ANTIBACTERIAL FOAMING SKIN CLEANSER- benzalkonium chloride soap 
Betco Corporation, Ltd.

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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E2 Antibacterial Foaming Skin Cleanser

E2 Antibacterial Foaming Skin Cleanser

​Active Ingredient

Benzalkonium Chloride 0.13%

E2 Antibacterial Foaming Skin Cleanser

Uses

  • For handwashing to decrease the bacteria on the skin.
  • Recommended for repeated use.

E2 Antibacterial Foaming Skin Cleanser

Warnings

  • For external use only.
  • When using this product avoid contact with eyes. In case of eye contact, flush eyes with water.
  • Stop use and ask a doctor If irritation persists or redness deelops, or if condition persists for more than 72 hours.
  • Keep out of reach of children.
  • If swallowed, get medical help or contact a Poison Control Center right away.

E2 Antibacterial Foaming Skin Cleanser

Directions

  • ​Read the entire label before using this product.
  • ​Dispense 2 pumps of product onto palm of hand and scrub thoroughly over all surfaces of both hands for 15 seconds. Rinse with clean water.

E2 Antibacterial Foaming Skin Cleanser

Inactive Ingredients

​Water, coco-glucoside, laurtrimonium chloride, cocamidopropylamine oxide, citric acid.

E2 Antibacterial Foaming Skin Cleanser

Purpose

Antimicrobial

E2 Antibacterial Foaming Skin Cleanser

KEEP OUT OF REACH OF CHILDREN

E2 Antibacterial Foaming Skin Cleanser

E2 Antibacterial Foaming Skin Cleanser

E2 rated antibacterial foaming skin cleanser for food service and Health care Applications.

2016 Betco Corporation

400 Van Camp Bowling Green, Ohio 43402

Made in U.S.A All rights reserved

888-GO-BETCO (888-462-3826)

Betco.com

750 mL (25.4 fl. oz.)

Item#717

SDS No. 717 717 label2.jpg

E2 ANTIBACTERIAL FOAMING SKIN CLEANSER 
benzalkonium chloride soap
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:65601-702
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE1.3 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
COCO GLUCOSIDE (UNII: ICS790225B)  
LAURTRIMONIUM CHLORIDE (UNII: A81MSI0FIC)  
COCAMIDOPROPYLAMINE OXIDE (UNII: M4SL82J7HK)  
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:65601-702-043780 mL in 1 BOTTLE; Type 0: Not a Combination Product09/15/201603/25/2019
2NDC:65601-702-291000 mL in 1 BAG; Type 0: Not a Combination Product09/15/201603/25/2019
3NDC:65601-702-03750 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product09/15/201603/25/2019
4NDC:65601-702-051250 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product09/15/201603/25/2019
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A09/15/201603/25/2019
Labeler - Betco Corporation, Ltd. (024492831)
Registrant - Betco corporation, Ltd. (024492831)
Establishment
NameAddressID/FEIBusiness Operations
Betco Corporation, Ltd.024492831manufacture(65601-702) , label(65601-702) , pack(65601-702)

Revised: 3/2019
Document Id: 84ef6f9a-ba34-66b1-e053-2991aa0a0c34
Set id: bc4cdb73-d30a-449c-af00-1e2c81d17a1c
Version: 4
Effective Time: 20190325
 
Betco Corporation, Ltd.